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Journal Abstract Search

97 related items for PubMed ID: 5173333

  • 1. Animal models of pigment and hearing abnormalities in man.
    Brown KS, Bergsma DR, Barrow MV.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):102-9. PubMed ID: 5173333
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  • 2. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):87-101. PubMed ID: 5006208
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  • 4. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
    Amini-Elihou S.
    J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
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  • 6. Penetrance and variability of major malformation syndromes associated with deafness.
    Pinsky L.
    Birth Defects Orig Artic Ser; 1979 Dec; 15(5B):207-26. PubMed ID: 393321
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  • 9. [Waardenburg's syndrome (type II) in 2 children, without parental involvement: genetic counseling].
    Dodinval P, Lhussier-Grodos TM.
    J Genet Hum; 1981 Sep; 29(3):273-84. PubMed ID: 7334349
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  • 12. Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III).
    Klein D.
    Am J Med Genet; 1983 Feb; 14(2):231-9. PubMed ID: 6340503
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  • 14. Waardenburg syndrome--penetrance of major signs.
    Preus M, Linstrom C, Polomeno RC, Milot J.
    Am J Med Genet; 1983 Jul; 15(3):383-8. PubMed ID: 6881207
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  • 15. [Make a diagnosis. Waardenburg's syndrome type 1].
    Aksu F.
    Padiatr Padol; 1983 Jul; 18(4):399-402. PubMed ID: 6646790
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  • 17. [Waardenburg's syndrome].
    Cacheux V, Delezoide AL, Vekemans M.
    C R Seances Soc Biol Fil; 1996 Jul; 190(5-6):577-80. PubMed ID: 9074723
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